Comparison of recovery profiles of propofol, dexmedetomidine, and remimazolam for monitored anesthetic care
- Conditions
- Not Applicable
- Registration Number
- KCT0006902
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
*ASA physical status 1-3
*age: 19-80 years
*patients who were scheduled to undergo upper limb surgery under brachial plexus block with monitored anesthetic care
* patients who refused to participate in this study
* patients with uncontrolled hypertension, hyperthyroidism, or moderate cardiac disease
* patients with severe hepatic/renal disease
* patients with chronic use of anti-depressant, anti-convulsant, psychotic drugs
* patients who abuses drugs or alcohol
* patients with severe obstructive sleep apnea
* patients with severe communicatino difficulties due to cognitive impairment
* patients with allergy to propofol, dexmedetomidine, or remimazolam
* patients who are judged inappropriate by attending anesthesiologists to participate in this study for other reasons
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time taken for MOAA/S to return to 5
- Secondary Outcome Measures
Name Time Method Alderete score;duration of brachial plexus block;time taken for MOAA/S to 3